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Study Summary: Nerve Block Treatment for Chronic Jaw Pain This study is being conducted at the TMJ (temporomandibular joint) clinic, which is part of the oral and maxillofacial surgery department. The goal is to evaluate how effective peripheral nerve blocks are in reducing long-term jaw pain in patients with chronic temporomandibular disorders (TMD) who haven't responded to at least two other types of treatment (such as physical therapy, medication, or bite splints).
What Is the Treatment? Peripheral nerve blocks are injections that temporarily block nerve signals from the painful area. This can relieve pain and improve function. These blocks are already used routinely at the clinic.
Who Can Join? Adults who have had jaw joint pain for over a year.
Have tried at least two other treatments without success.
Are mentally competent and not pregnant.
What Will Participation Involve? You'll receive the nerve block treatment as part of your regular care.
You'll be asked to attend follow-up visits, typically one every 4 months (3 per year).
You'll be monitored for pain relief, mouth opening ability, and use of pain medications.
You can stop participating at any time without affecting your care.
How Will Data Be Handled? Your information will be stored securely and coded to protect your identity.
Only the research team will have access to your personal information.
How Many People Will Be in the Study? The goal is to recruit 40 patients.
Full description
Background:
Chronic temporomandibular disorders (TMD) are a common source of orofacial pain, affecting both younger and older populations. Symptoms often include sharp, persistent pain in the temporomandibular joint (TMJ) region, difficulty opening or closing the mouth, and functional limitations in the jaw and facial muscles. The condition may arise from various causes, including trauma, genetic predisposition, and muscular or joint stress.
Conventional treatments-such as medications, physiotherapy, bite splints, and complementary therapies-offer relief to many patients, but a subset remains resistant to these modalities. In recent years, peripheral nerve blocks have emerged as a promising intervention for managing chronic TMD-related pain, particularly in patients unresponsive to standard care.
Purpose of the Study:
This prospective observational study aims to systematically assess the effectiveness of peripheral nerve blocks as a treatment for chronic temporomandibular pain. The intervention is already part of routine clinical care in the TMJ clinic, and this study will evaluate patient outcomes in a structured manner.
Study Design and Methods:
Patients attending the TMJ clinic at our institution, who meet specific inclusion criteria, will be invited to participate in a follow-up study after receiving a peripheral nerve block as part of their clinical care. The treatment involves injecting anesthetic near specific nerves to block pain signals from the TMJ region.
Data will be collected prospectively from up to 40 adult participants. Baseline and follow-up data will include:
Pain levels (using the Visual Analog Scale - VAS)
Mouth opening range (in millimeters)
Changes in the use of pain medication
Whether the patient requests repeat treatments
Demographics and relevant medical background (age, sex, comorbidities, previous treatments, physical activity)
Follow-up visits will occur as per the clinic's standard practice, typically every four months (total of three visits per year), with the possibility for earlier visits if symptoms worsen. Patients must attend at least two follow-up visits within four months post-injection to remain in the study.
Inclusion Criteria:
Adults (non-pregnant) with sound judgment
Chronic TMJ pain lasting at least 12 months
Documented failure of at least two previous treatment modalities
Exclusion Criteria:
Failure to meet inclusion criteria
Missing at least two follow-up visits within the specified timeframe
Data Handling and Confidentiality:
All data will be anonymized and stored in a secure, password-protected Excel file within the department. Only approved researchers will have access. Patient identifiers will be replaced with study codes. No personal identifying information will be published or disclosed.
Ethical Considerations:
The study will only begin after approval by the institutional Helsinki (ethics) committee. All participants will provide written informed consent after receiving a thorough explanation of the study. Participation is voluntary and will not impact the quality or accessibility of their medical care. Patients may withdraw at any time without consequence.
Statistical Analysis:
The main outcomes (VAS scores, analgesic use, and mouth opening) will be compared before and after treatment using standard statistical methods. Subgroup analyses will explore correlations between outcomes and demographic/clinical variables such as age, sex, and previous treatment history.
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Data sourced from clinicaltrials.gov
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